A periodontal cleaning device, including a cleaning head having a fluid outlet for releasing a cleaning fluid and a suction member for suction of a waste fluid, a cleaning fluid source, connected to the fluid outlet, a controllable suction device connected to the suction member, fluid feeding device for controlling a flow of the cleaning fluid from the cleaning fluid source to the fluid outlet. The periodontal cleaning device further has a control unit, arranged for controlling the controllable suction device in generating a vacuum pulse in the suction member, controlling controllable fluid feeding device in generating a fluid flow pulse in the fluid outlet in response to the vacuum pulse, and controlling the controllable suction device in generating a subsequent vacuum pulse in the suction member, and introducing a time period between the cleaning fluid flow pulse and the subsequent vacuum pulse in the suction member.

Aspiration systems and methods for controlling blood loss during thrombus removal are disclosed herein. The systems include an aspiration catheter, an aspiration tubing, a receptacle for collecting aspirated blood, a vacuum line coupled to the receptacle, and a sensor configured to measure a flow parameter associated with a liquid within an aspiration lumen. The systems further include a regulator configured to adjust a vacuum pressure within the vacuum line, and a vacuum controller operably coupled to the sensor and the regulator. The vacuum controller is configured to receive the flow parameter from the sensor, compare the flow parameter to a target range for the flow parameter, and send an automatic control signal to the regulator based on a comparison of the flow parameter to the target range. The automatic control signal causes the regulator to adjust the vacuum pressure within the vacuum line.

An all-in-one, sterile, waste- and mess-free device for cleaning two-sided bodily punctures is described. The device may be a hand-held device that encloses around both sides of a two-sided bodily puncture and provides targeted cleaning fluid soaking, fully or partially submerged, without the user ever needing to touch or disturb jewelry in the two-sided bodily puncture. Cleaning fluid soaking involves cleaning fluid, without elevated pressure, soakingly contacting a two-sided bodily puncture to: (1) kill microorganisms in the area surrounding the two-sided bodily puncture (e.g., skin surrounding openings of the two-sided bodily puncture); and/or (2) remove cellular debris and/or microorganisms from the area surrounding the two-sided bodily puncture.

Disclosed are saliva collection containers comprising a removable cartridge containing a liquid absorbent material, the removable cartridge adapted to receive saliva from a user; a suction source removably disposed therein and fluidly coupled to the removable cartridge, wherein the saliva collection container is adapted to receive the removable cartridge; and a tubing having a first end and second end opposite of the first end, wherein the first end of the tubing is fluidly coupled to the suction source through an opening in the neck of the saliva collection container. Disclosed are saliva collection containers comprising a cartridge containing a liquid absorbent material, the cartridge adapted to fit inside a tubing; a tubing having a first end and second end opposite of the first end, wherein the first end of the tubing is fluidly coupled to the suction source; wherein the tubing is adapted to receive the cartridge; and a suction source removably disposed therein and fluidly coupled to the tubing.

A device suitable for collecting and transporting urine away from the body of a person including a casing defining an internal volume and an opening. The casing can include a compressible material which is elastically deformable when the device is disposed in a pubic region of a female user. The device can include a porous material disposed within the internal volume and in fluid communication with the opening. The porous material can wick, draw, or direct fluid, such as urine, away from the pubic region of the female user and into the internal volume. The device can include a fluid conduit disposed within the internal volume and enabling extraction of fluid from the internal volume. The device can include a fluid impermeable housing disposed within the internal volume and adhered or otherwise affixed to the casing.

Examples relate to fluid collection assemblies, systems, and methods for collecting fluid from a wearer of the fluid collection assembly. The fluid collection assemblies include a fluid collection device attachable to an adapter. The fluid collection device includes porous material disposed within a fluid impermeable barrier. The adapter includes an interfacing body having at least one orifice and at least one attachment feature for attaching the adapter to the fluid collection device such that the porous material is fluidly connected to the at least one orifice. A fluid collection system includes a fluid collection device operably coupled to a fluid storage container and vacuum source via one or more sections of conduit.

A vacuum regulator device having a vacuum regulator and a vacuum gauge on a housing line that is configured to be in fluid communication with a patient include an electronic valve that selectively opens and closes the housing line. The vacuum gauge is located between the vacuum regulator and the patient and includes an electronic flow sensor upstream. The electronic flow sensor provides feedback to the vacuum regulator.

Methods for operating a medical waste collection system. The medical waste collection system includes a waste canister, a vacuum source, a user interface, and a controller. The controller operates the vacuum source so that an actual vacuum level does not exceed a suction limit set by the user through the user interface. A suction limit lock may be activated to permit the user to adjust the suction limit up to the suction limit lock and to prevent the user from adjusting the suction limit above the suction limit lock. If the user provides an input that indicates an attempt to adjust the suction limit above a selected vacuum level associated with the suction limit lock, then the user interface may display a prompt with an option to disable the suction limit lock.

A wound therapy device and method includes a skin contacting element, a reactor, and a reactor housing element. The skin contacting element is configured for covering an associated tissue site, the reactor for creating a pressure condition at the associated tissue site upon actuation thereof, and the reactor housing element for accommodating the reactor. The skin contacting element has a skin contacting side and an interface side, which is opposite the skin contacting side. The reactor housing element has a lower affixing side and an upper side, which is opposite the lower affixing side.

A negative pressure wound therapy device that includes a first tubing connectable in flow communication with a source of negative pressure configured for application of negative pressure to a wound site, a second tubing in flow communication with the wound site, and a valve.